Clinical Research Assistant (Part Time)

Tidewater Physicians Multispecialty Group P C•Newport News, VA

About The Position

The Clinical Research Assistant will be responsible for performing duties as assigned according to these standards. Candidates with experience working in a research setting are preferred. A knowledge of medical terminology is essential.

Requirements

  • Knowledge of medical terminology to include symptomology, diagnoses, medications, anatomy and standard medical equipment and procedures.
  • Ability to work scheduled hours as defined in the job offer.
  • Must be able to work flexible hours
  • Ability to understand information on trial protocols, technical sites, government regulations and others whether presented in written or other formats.
  • Must have excellent interpersonal skills with subjects/patients, staff and all health care professionals with excellent verbal and written communication skills, consistent professional conduct, and meticulous attention to detail.
  • Must become familiar with the Clinical Research department’s SOP’s and study protocols, and is responsible for following these.
  • Current College student, Recent Graduate or associate degree or equivalent; preferably in the sciences.
  • Current driver’s license and transportation.

Nice To Haves

  • Experience working in a research setting are preferred.
  • Preferred experience in a clinical healthcare position; previous Nursing, Medical Assistant or Phlebotomy experience.
  • Experience with EHR preferred.
  • Previous experience with clinical trials a plus.

Responsibilities

  • Assess eligibility of potential subjects through review of medical records and discussion of patient status with the Medical Director, the Principal Investigator, other Investigators, nurses and/or the CRC as appropriate.
  • Schedule subjects for appointments or procedures as directed to meet study protocols.
  • Collect, maintain, and enter data in keeping with the requirements of the department and the particular study as required; this may be electronic or printed based on requirements of the study.
  • Assist with collection, processing, and shipping of blood/urine specimens at scheduled patient visits.
  • Administer questionnaires/diaries per protocol.
  • Assist the CRC in the performance of other study related duties and general office support as instructed.
  • Other duties as assigned.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service